Secreted Factors from Stem Cells of Human Exfoliated Deciduous Teeth Directly Activate Endothelial Cells to Promote All Processes of Angiogenesis

• Published in: Cells (Basel, Switzerland) Vol. 9; no. 11; p. 2385
• Main Authors: Kato, Makoto, Tsunekawa, Shin, Nakamura, Nobuhisa, Miura-Yura, Emiri, Yamada, Yuichiro, Hayashi, Yusuke, Nakai-Shimoda, Hiromi, Asano, Saeko, Hayami, Tomohide, Motegi, Mikio, Asano-Hayami, Emi, Sasajima, Sachiko, Morishita, Yoshiaki, Himeno, Tatsuhito, Kondo, Masaki, Kato, Yoshiro, Izumoto-Akita, Takako, Yamamoto, Akihito, Naruse, Keiko, Nakamura, Jiro, Kamiya, Hideki
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 31.10.2020; MDPI
• Subjects: angiogenesis; conditioned medium; endothelial cell; Endothelium; Neovascularization; Observations; Physiological aspects; SHED; Stem cells; Japan; conditioned medium; SHED; angiogenesis; endothelial cell
• ISSN: 2073-4409; 2073-4409
• DOI: 10.3390/cells9112385

Diabetes is a major risk factor for atherosclerosis and ischemic vascular diseases. Recently, regenerative medicine is expected to be a novel therapy for ischemic diseases. Our previous studies have reported that transplantation of stem cells promoted therapeutic angiogenesis for diabetic neuropathy and ischemic vascular disease in a paracrine manner, but the precise mechanism is unclear. Therefore, we examined whether secreted factors from stem cells had direct beneficial effects on endothelial cells to promote angiogenesis. The soluble factors were collected as conditioned medium (CM) 48 h after culturing stem cells from human exfoliated deciduous teeth (SHED) in serum-free DMEM. SHED-CM significantly increased cell viability of human umbilical vein endothelial cells (HUVECs) in MTT assays and accelerated HUVECs migration in wound healing and Boyden chamber assays. In a Matrigel plug assay of mice, the migrated number of primary endothelial cells was markedly increased in the plug containing SHED-CM or SHED suspension. SHED-CM induced complex tubular structures of HUVECs in a tube formation assay. Furthermore, SHED-CM significantly increased neovascularization from the primary rat aorta, indicating that SHED-CM stimulated primary endothelial cells to promote comprehensive angiogenesis processes. The angiogenic effects of SHED-CM were the same or greater than the effective concentration of VEGF. In conclusion, SHED-CM directly stimulates vascular endothelial cells to promote angiogenesis and is promising for future clinical application.